Cargando…

Influence of timing on CSF tests value for Creutzfeldt-Jakob disease diagnosis

BACKGROUND: The analysis of markers in the cerebrospinal fluid (CSF) is useful in the diagnosis of sporadic Creutzfeldt-Jakob disease (sCJD). However, the time at which the study of these markers is most sensitive remains controversal. OBJECTIVE: To assess the influence of time of sampling on the va...

Descripción completa

Detalles Bibliográficos
Autores principales:	Sanchez-Juan, P., Sánchez-Valle, R., Green, A., Ladogana, A., Cuadrado-Corrales, N., Mitrová, E., Stoeck, K., Sklaviadis, T., Kulczycki, J., Hess, K., Krasnianski, A., Equestre, M., Slivarichová, D., Saiz, A., Calero, M., Pocchiari, M., Knight, R., van Duijn, C. M., Zerr, I.
Formato:	Texto
Lenguaje:	English
Publicado:	Steinkopff-Verlag 2007
Materias:	Original Communication
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2779401/ https://www.ncbi.nlm.nih.gov/pubmed/17385081 http://dx.doi.org/10.1007/s00415-006-0472-9

Ejemplares similares

Cerebrospinal fluid biomarker supported diagnosis of Creutzfeldt–Jakob disease and rapid dementias: a longitudinal multicentre study over 10 years
por: Stoeck, Katharina, et al.
Publicado: (2012)

Cerebrospinal fluid biomarkers in human genetic transmissible spongiform encephalopathies
por: Ladogana, Anna, et al.
Publicado: (2009)

The importance of ongoing international surveillance for Creutzfeldt–Jakob disease
por: Watson, Neil, et al.
Publicado: (2021)

Updated clinical diagnostic criteria for sporadic Creutzfeldt-Jakob disease
por: Zerr, I., et al.
Publicado: (2009)

Neurofilaments in blood and CSF for diagnosis and prediction of onset in Creutzfeldt-Jakob disease
por: Steinacker, Petra, et al.
Publicado: (2016)

Iatrogenic Creutzfeldt-Jakob Disease, Final Assessment
por: Brown, Paul, et al.
Publicado: (2012)

Validation of Revised International Creutzfeldt-Jakob Disease Surveillance Network Diagnostic Criteria for Sporadic Creutzfeldt-Jakob Disease
por: Watson, Neil, et al.
Publicado: (2022)

Diagnostic Accuracy of Prion Disease Biomarkers in Iatrogenic Creutzfeldt-Jakob Disease
por: Llorens, Franc, et al.
Publicado: (2020)

Validation of α-Synuclein as a CSF Biomarker for Sporadic Creutzfeldt-Jakob Disease
por: Llorens, Franc, et al.
Publicado: (2017)

A Genome Wide Association Study Links Glutamate Receptor Pathway to Sporadic Creutzfeldt-Jakob Disease Risk
por: Sanchez-Juan, Pascual, et al.
Publicado: (2015)

Incidence and spectrum of sporadic Creutzfeldt–Jakob disease variants with mixed phenotype and co-occurrence of PrP(Sc) types: an updated classification
por: Parchi, Piero, et al.
Publicado: (2009)

Revisiting the Heidenhain Variant of Creutzfeldt-Jakob Disease: Evidence for Prion Type Variability Influencing Clinical Course and Laboratory Findings
por: Baiardi, Simone, et al.
Publicado: (2015)

Age at Death of Creutzfeldt-Jakob Disease in Subsequent Family Generation Carrying the E200K Mutation of the Prion Protein Gene
por: Pocchiari, Maurizio, et al.
Publicado: (2013)

Extended and direct evaluation of RT‐QuIC assays for Creutzfeldt‐Jakob disease diagnosis
por: Groveman, Bradley R., et al.
Publicado: (2016)

Clinical aspects of common genetic Creutzfeldt-Jakob disease
por: Schelzke, Gabi, et al.
Publicado: (2012)

Source of Variant Creutzfeldt-Jakob Disease outside United Kingdom
por: Sanchez-Juan, Pascual, et al.
Publicado: (2007)

Biochemical and Neuropathological Findings in a Creutzfeldt–Jakob Disease Patient with the Rare Val180Ile-129Val Haplotype in the Prion Protein Gene
por: Zanusso, Gianluigi, et al.
Publicado: (2022)

The first case of variant Creutzfeldt-Jakob disease in the Netherlands
por: Sánchez-Juan, P., et al.
Publicado: (2007)

Stability and Reproducibility Underscore Utility of RT-QuIC for Diagnosis of Creutzfeldt-Jakob Disease
por: Cramm, Maria, et al.
Publicado: (2015)

Genetic Risk Factors of Creutzfeldt-Jakob Disease in the Population of Newborns in Slovakia
por: Kosorinova, Dana, et al.
Publicado: (2021)

Sporadic Creutzfeldt–Jakob disease subtype-specific alterations of the brain proteome: Impact on Rab3a recycling
por: Gawinecka, Joanna, et al.
Publicado: (2012)

Immune responses in rapidly progressive dementia: a comparative study of neuroinflammatory markers in Creutzfeldt-Jakob disease, Alzheimer’s disease and multiple sclerosis
por: Stoeck, Katharina, et al.
Publicado: (2014)

Ocular Dipping in Creutzfeldt-Jakob Disease
por: Sierra-Hidalgo, Fernando, et al.
Publicado: (2014)

Prion-specific and surrogate CSF biomarkers in Creutzfeldt-Jakob disease: diagnostic accuracy in relation to molecular subtypes and analysis of neuropathological correlates of p-tau and Aβ42 levels
por: Lattanzio, Francesca, et al.
Publicado: (2017)

Clinicopathological features of the rare form of Creutzfeldt-Jakob disease in R208H-V129V PRNP carrier
por: Tiple, Dorina, et al.
Publicado: (2019)

Etymologia: Creutzfeldt-Jakob Disease
por: Henry, Ronnie, et al.
Publicado: (2017)

Blood Transfusion and Spread of Variant Creutzfeldt-Jakob Disease
por: Dietz, Klaus, et al.
Publicado: (2007)

Role of different recombinant PrP substrates in the diagnostic accuracy of the CSF RT-QuIC assay in Creutzfeldt-Jakob disease
por: Da Silva Correia, Susana Margarida, et al.
Publicado: (2022)

Creutzfeldt-Jakob dementia
por: Reis, Fabiano, et al.
Publicado: (2015)

Prodynorphin and Proenkephalin in Cerebrospinal Fluid of Sporadic Creutzfeldt–Jakob Disease
por: Abu-Rumeileh, Samir, et al.
Publicado: (2022)

CSF SerpinA1 in Creutzfeldt–Jakob disease and frontotemporal lobar degeneration
por: Abu‐Rumeileh, Samir, et al.
Publicado: (2020)

A polymorphism in the regulatory region of PRNP is associated with increased risk of sporadic Creutzfeldt-Jakob disease
por: Sanchez-Juan, Pascual, et al.
Publicado: (2011)

Subtype and Regional-Specific Neuroinflammation in Sporadic Creutzfeldt–Jakob Disease
por: Llorens, Franc, et al.
Publicado: (2014)

Efficient Transmission and Characterization of Creutzfeldt–Jakob Disease Strains in Bank Voles
por: Nonno, Romolo, et al.
Publicado: (2006)

Cerebrospinal fluid real‐time quaking‐induced conversion is a robust and reliable test for sporadic creutzfeldt–jakob disease: An international study
por: McGuire, Lynne I., et al.
Publicado: (2016)

No evidence for association between tau gene haplotypic variants and susceptibility to Creutzfeldt-Jakob disease
por: Sánchez-Juan, Pascual, et al.
Publicado: (2007)

Treating seizures in Creutzfeldt–Jakob disease()
por: Ng, Marcus C., et al.
Publicado: (2014)

Assessing Prion Infectivity of Human Urine in Sporadic Creutzfeldt-Jakob Disease
por: Notari, Silvio, et al.
Publicado: (2012)

Is Creutzfeldt-Jakob disease transmitted in blood?
por: Ricketts, M N, et al.
Publicado: (1997)

A case of Creutzfeldt-Jakob disease.
por: Cha, J. K., et al.
Publicado: (1991)

Cannot write session to /tmp/vufind_sessions/sess_37njflh31l9u1k95u81g6bc4oo